Zenchent
Zenchent® 0.4/35 (Norethindrone and Ethinyl Estradiol Tablets USP, 0.4 mg/0.035 mg, 28-Day)
Approved
Approval ID
3c247e9d-fff8-40e8-a9d3-88adee3426e2
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 13, 2010
Manufacturers
FDA
Physicians Total Care, Inc.
DUNS: 194123980
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Norethindrone and Ethinyl Estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-6273
Application NumberANDA078323
Product Classification
M
Marketing Category
C73584
G
Generic Name
Norethindrone and Ethinyl Estradiol
Product Specifications
Effective DateJuly 5, 2011
FDA Product Classification